Consolidating Lithiothermic-Ready Transition Metals for Li2 S-Based Cathodes
© 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
Veröffentlicht in: | Advanced materials (Deerfield Beach, Fla.). - 1998. - 32(2020), 31 vom: 26. Aug., Seite e2002403 |
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1. Verfasser: | |
Weitere Verfasser: | , , , , , , , , , , , |
Format: | Online-Aufsatz |
Sprache: | English |
Veröffentlicht: |
2020
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Zugriff auf das übergeordnete Werk: | Advanced materials (Deerfield Beach, Fla.) |
Schlagworte: | Journal Article LiS bonds activation potential lithiothermic reactions lithium sulfide transition metals |
Zusammenfassung: | © 2020 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. Li2 S holds a promising role as a high-capacity Li-containing cathode, circumventing use of metallic lithium in constructing next-generation batteries to replace current Li-ion batteries. However, progress of Li2 S cathode has been plagued by its intrinsic drawbacks, including high activation potentials, poor rate performance, and rapid capacity fading during long cycling. Herein, a series of Li2 S/transition metal (TM) nanocomposites are synthesized via a lithiothermic reduction reaction, and it is realized that the presence of TMs in Li2 S matrix can transform electrochemical behaviors of Li2 S. On the one hand, the incorporation of W, Mo, or Ti greatly increases electronic and ionic conductivity of Li2 S composites and inhibits the polysulfide dissolution via the TMS bond, effectively addressing the drawbacks of Li2 S cathodes. In particular, Li2 S/W and Li2 S/Mo exhibit the highest ionic conductivity of solid-phase Li-ion conductors ever-reported: 5.44 × 10-2 and 3.62 × 10-2 S m-1 , respectively. On the other hand, integrating Co, Mn, and Zn turns Li2 S into a prelithiation agent, forming metal sulfides rather than S8 after the full charge. These interesting findings may shed light on the design of Li2 S-based cathode materials |
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Beschreibung: | Date Revised 30.09.2020 published: Print-Electronic Citation Status PubMed-not-MEDLINE |
ISSN: | 1521-4095 |
DOI: | 10.1002/adma.202002403 |